Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4HJ30
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006399 | tRNA metabolic process | 7 | 1 |
GO:0006400 | tRNA modification | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008033 | tRNA processing | 8 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009451 | RNA modification | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0030488 | tRNA methylation | 5 | 1 |
GO:0032259 | methylation | 2 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043414 | macromolecule methylation | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0008168 | methyltransferase activity | 4 | 11 |
GO:0008171 | O-methyltransferase activity | 5 | 11 |
GO:0008173 | RNA methyltransferase activity | 4 | 11 |
GO:0008175 | tRNA methyltransferase activity | 5 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0062105 | RNA 2'-O-methyltransferase activity | 5 | 11 |
GO:0106050 | tRNA 2'-O-methyltransferase activity | 6 | 11 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 11 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 11 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 29 | 33 | PF00656 | 0.486 |
CLV_NRD_NRD_1 | 109 | 111 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.266 |
CLV_NRD_NRD_1 | 498 | 500 | PF00675 | 0.251 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 656 | 658 | PF00675 | 0.298 |
CLV_NRD_NRD_1 | 660 | 662 | PF00675 | 0.298 |
CLV_NRD_NRD_1 | 676 | 678 | PF00675 | 0.150 |
CLV_PCSK_FUR_1 | 126 | 130 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 109 | 111 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 498 | 500 | PF00082 | 0.242 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 656 | 658 | PF00082 | 0.252 |
CLV_PCSK_KEX2_1 | 664 | 666 | PF00082 | 0.228 |
CLV_PCSK_KEX2_1 | 676 | 678 | PF00082 | 0.150 |
CLV_PCSK_PC1ET2_1 | 120 | 122 | PF00082 | 0.508 |
CLV_PCSK_PC1ET2_1 | 664 | 666 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 285 | 289 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 526 | 530 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 690 | 694 | PF00082 | 0.255 |
DEG_APCC_DBOX_1 | 485 | 493 | PF00400 | 0.501 |
DEG_APCC_DBOX_1 | 525 | 533 | PF00400 | 0.576 |
DEG_APCC_DBOX_1 | 602 | 610 | PF00400 | 0.455 |
DEG_APCC_DBOX_1 | 63 | 71 | PF00400 | 0.444 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.434 |
DEG_SCF_FBW7_1 | 346 | 351 | PF00400 | 0.497 |
DEG_SCF_FBW7_2 | 342 | 349 | PF00400 | 0.507 |
DOC_CKS1_1 | 465 | 470 | PF01111 | 0.461 |
DOC_CYCLIN_yCln2_LP_2 | 74 | 77 | PF00134 | 0.422 |
DOC_MAPK_FxFP_2 | 41 | 44 | PF00069 | 0.420 |
DOC_MAPK_gen_1 | 128 | 137 | PF00069 | 0.521 |
DOC_MAPK_gen_1 | 504 | 512 | PF00069 | 0.457 |
DOC_MAPK_gen_1 | 661 | 672 | PF00069 | 0.465 |
DOC_MAPK_gen_1 | 676 | 683 | PF00069 | 0.428 |
DOC_MAPK_MEF2A_6 | 128 | 137 | PF00069 | 0.523 |
DOC_MAPK_MEF2A_6 | 418 | 425 | PF00069 | 0.380 |
DOC_MAPK_MEF2A_6 | 486 | 494 | PF00069 | 0.504 |
DOC_MAPK_MEF2A_6 | 665 | 674 | PF00069 | 0.536 |
DOC_PP1_RVXF_1 | 430 | 436 | PF00149 | 0.384 |
DOC_PP1_RVXF_1 | 669 | 675 | PF00149 | 0.536 |
DOC_PP2B_LxvP_1 | 622 | 625 | PF13499 | 0.475 |
DOC_PP2B_LxvP_1 | 74 | 77 | PF13499 | 0.422 |
DOC_PP4_FxxP_1 | 137 | 140 | PF00568 | 0.522 |
DOC_PP4_FxxP_1 | 41 | 44 | PF00568 | 0.420 |
DOC_PP4_FxxP_1 | 86 | 89 | PF00568 | 0.444 |
DOC_PP4_FxxP_1 | 95 | 98 | PF00568 | 0.450 |
DOC_PP4_MxPP_1 | 609 | 612 | PF00568 | 0.384 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.777 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 471 | 475 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 534 | 538 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 625 | 629 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 638 | 642 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.541 |
DOC_USP7_MATH_2 | 348 | 354 | PF00917 | 0.489 |
DOC_USP7_UBL2_3 | 120 | 124 | PF12436 | 0.511 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.754 |
DOC_WW_Pin1_4 | 461 | 466 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.567 |
LIG_14-3-3_CanoR_1 | 182 | 190 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 259 | 268 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 295 | 303 | PF00244 | 0.393 |
LIG_14-3-3_CanoR_1 | 379 | 388 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 398 | 406 | PF00244 | 0.680 |
LIG_14-3-3_CanoR_1 | 504 | 512 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 526 | 536 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 656 | 660 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 99 | 103 | PF00244 | 0.473 |
LIG_Actin_WH2_2 | 245 | 261 | PF00022 | 0.498 |
LIG_APCC_ABBAyCdc20_2 | 403 | 409 | PF00400 | 0.306 |
LIG_BRCT_BRCA1_1 | 45 | 49 | PF00533 | 0.428 |
LIG_Clathr_ClatBox_1 | 489 | 493 | PF01394 | 0.473 |
LIG_CSL_BTD_1 | 137 | 140 | PF09270 | 0.473 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.476 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.485 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.680 |
LIG_FHA_1 | 438 | 444 | PF00498 | 0.538 |
LIG_FHA_1 | 687 | 693 | PF00498 | 0.530 |
LIG_FHA_2 | 145 | 151 | PF00498 | 0.613 |
LIG_FHA_2 | 295 | 301 | PF00498 | 0.475 |
LIG_FHA_2 | 345 | 351 | PF00498 | 0.767 |
LIG_FHA_2 | 453 | 459 | PF00498 | 0.384 |
LIG_FHA_2 | 628 | 634 | PF00498 | 0.534 |
LIG_FHA_2 | 686 | 692 | PF00498 | 0.498 |
LIG_HP1_1 | 488 | 492 | PF01393 | 0.536 |
LIG_Integrin_RGD_1 | 228 | 230 | PF01839 | 0.543 |
LIG_LIR_Apic_2 | 38 | 44 | PF02991 | 0.426 |
LIG_LIR_Apic_2 | 94 | 98 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 38 | 47 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 409 | 416 | PF02991 | 0.403 |
LIG_LIR_Gen_1 | 474 | 484 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 556 | 565 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 628 | 639 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 169 | 175 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 38 | 42 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 409 | 414 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 474 | 480 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 556 | 561 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 633 | 639 | PF02991 | 0.459 |
LIG_Pex14_2 | 39 | 43 | PF04695 | 0.434 |
LIG_Pex14_2 | 45 | 49 | PF04695 | 0.417 |
LIG_PTAP_UEV_1 | 467 | 472 | PF05743 | 0.401 |
LIG_SH2_NCK_1 | 355 | 359 | PF00017 | 0.473 |
LIG_SH2_STAP1 | 244 | 248 | PF00017 | 0.442 |
LIG_SH2_STAP1 | 317 | 321 | PF00017 | 0.406 |
LIG_SH2_STAT3 | 260 | 263 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 680 | 683 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 687 | 690 | PF00017 | 0.450 |
LIG_SH3_3 | 110 | 116 | PF00018 | 0.531 |
LIG_SH3_3 | 158 | 164 | PF00018 | 0.736 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.304 |
LIG_SH3_3 | 462 | 468 | PF00018 | 0.576 |
LIG_SH3_3 | 586 | 592 | PF00018 | 0.519 |
LIG_SH3_3 | 70 | 76 | PF00018 | 0.443 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.446 |
LIG_SUMO_SIM_anti_2 | 324 | 329 | PF11976 | 0.511 |
LIG_SUMO_SIM_par_1 | 487 | 493 | PF11976 | 0.444 |
LIG_SUMO_SIM_par_1 | 53 | 60 | PF11976 | 0.448 |
LIG_SUMO_SIM_par_1 | 578 | 585 | PF11976 | 0.554 |
LIG_SUMO_SIM_par_1 | 592 | 598 | PF11976 | 0.527 |
LIG_TRAF2_1 | 347 | 350 | PF00917 | 0.645 |
LIG_TRAF2_2 | 164 | 169 | PF00917 | 0.377 |
MOD_CDK_SPK_2 | 155 | 160 | PF00069 | 0.513 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.565 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.626 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.350 |
MOD_CK1_1 | 438 | 444 | PF00069 | 0.419 |
MOD_CK1_1 | 464 | 470 | PF00069 | 0.558 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.497 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.546 |
MOD_CK1_1 | 575 | 581 | PF00069 | 0.467 |
MOD_CK1_1 | 641 | 647 | PF00069 | 0.448 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.715 |
MOD_CK2_1 | 243 | 249 | PF00069 | 0.546 |
MOD_CK2_1 | 344 | 350 | PF00069 | 0.731 |
MOD_CK2_1 | 439 | 445 | PF00069 | 0.552 |
MOD_CK2_1 | 627 | 633 | PF00069 | 0.467 |
MOD_Cter_Amidation | 659 | 662 | PF01082 | 0.296 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.711 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.595 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.521 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.671 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.707 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.283 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.431 |
MOD_GlcNHglycan | 536 | 539 | PF01048 | 0.333 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.758 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.615 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.518 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.752 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.494 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.580 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.664 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.522 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.458 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.559 |
MOD_GSK3_1 | 625 | 632 | PF00069 | 0.495 |
MOD_GSK3_1 | 686 | 693 | PF00069 | 0.535 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.494 |
MOD_N-GLC_1 | 239 | 244 | PF02516 | 0.242 |
MOD_N-GLC_2 | 171 | 173 | PF02516 | 0.244 |
MOD_N-GLC_2 | 696 | 698 | PF02516 | 0.255 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.638 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.474 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.586 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.705 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.401 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.489 |
MOD_NEK2_1 | 572 | 577 | PF00069 | 0.455 |
MOD_NEK2_2 | 471 | 476 | PF00069 | 0.384 |
MOD_OFUCOSY | 569 | 576 | PF10250 | 0.273 |
MOD_PIKK_1 | 162 | 168 | PF00454 | 0.659 |
MOD_PIKK_1 | 183 | 189 | PF00454 | 0.384 |
MOD_PIKK_1 | 259 | 265 | PF00454 | 0.424 |
MOD_PIKK_1 | 290 | 296 | PF00454 | 0.603 |
MOD_PIKK_1 | 364 | 370 | PF00454 | 0.536 |
MOD_PIKK_1 | 398 | 404 | PF00454 | 0.622 |
MOD_PIKK_1 | 452 | 458 | PF00454 | 0.453 |
MOD_PIKK_1 | 582 | 588 | PF00454 | 0.515 |
MOD_PK_1 | 299 | 305 | PF00069 | 0.307 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.419 |
MOD_PKA_2 | 397 | 403 | PF00069 | 0.584 |
MOD_PKA_2 | 505 | 511 | PF00069 | 0.438 |
MOD_PKA_2 | 655 | 661 | PF00069 | 0.477 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.469 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.442 |
MOD_Plk_1 | 299 | 305 | PF00069 | 0.307 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.536 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.432 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.442 |
MOD_Plk_4 | 350 | 356 | PF00069 | 0.483 |
MOD_Plk_4 | 390 | 396 | PF00069 | 0.590 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.695 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.677 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.752 |
MOD_ProDKin_1 | 461 | 467 | PF00069 | 0.582 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.566 |
MOD_SUMO_rev_2 | 269 | 274 | PF00179 | 0.377 |
TRG_DiLeu_BaEn_1 | 579 | 584 | PF01217 | 0.384 |
TRG_DiLeu_BaEn_1 | 695 | 700 | PF01217 | 0.384 |
TRG_ENDOCYTIC_2 | 680 | 683 | PF00928 | 0.536 |
TRG_ER_diArg_1 | 121 | 123 | PF00400 | 0.582 |
TRG_ER_diArg_1 | 126 | 129 | PF00400 | 0.548 |
TRG_ER_diArg_1 | 497 | 499 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 514 | 517 | PF00400 | 0.464 |
TRG_ER_diArg_1 | 675 | 677 | PF00400 | 0.568 |
TRG_NLS_Bipartite_1 | 109 | 124 | PF00514 | 0.496 |
TRG_NLS_MonoExtC_3 | 119 | 124 | PF00514 | 0.509 |
TRG_NLS_MonoExtC_3 | 660 | 665 | PF00514 | 0.496 |
TRG_NLS_MonoExtN_4 | 117 | 124 | PF00514 | 0.501 |
TRG_Pf-PMV_PEXEL_1 | 299 | 304 | PF00026 | 0.382 |
TRG_Pf-PMV_PEXEL_1 | 379 | 383 | PF00026 | 0.484 |
TRG_Pf-PMV_PEXEL_1 | 665 | 669 | PF00026 | 0.330 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMP0 | Leptomonas seymouri | 56% | 100% |
A0A1X0NKZ4 | Trypanosomatidae | 37% | 100% |
A0A3Q8IFC1 | Leishmania donovani | 77% | 100% |
A0A3R7N0X9 | Trypanosoma rangeli | 41% | 100% |
A4I6K9 | Leishmania infantum | 77% | 100% |
C9ZN61 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9B1K2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
Q4Q6L1 | Leishmania major | 75% | 100% |
V5BII3 | Trypanosoma cruzi | 41% | 100% |