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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AKK7
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 10 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006396 | RNA processing | 6 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009451 | RNA modification | 5 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016070 | RNA metabolic process | 5 | 10 |
GO:0032259 | methylation | 2 | 10 |
GO:0034470 | ncRNA processing | 7 | 10 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0034660 | ncRNA metabolic process | 6 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0043412 | macromolecule modification | 4 | 10 |
GO:0043414 | macromolecule methylation | 3 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 10 |
GO:0046483 | heterocycle metabolic process | 3 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0090304 | nucleic acid metabolic process | 4 | 10 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0008168 | methyltransferase activity | 4 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0004809 | tRNA (guanine-N2-)-methyltransferase activity | 6 | 1 |
GO:0008170 | N-methyltransferase activity | 5 | 1 |
GO:0008173 | RNA methyltransferase activity | 4 | 1 |
GO:0008175 | tRNA methyltransferase activity | 5 | 1 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 1 |
GO:0016423 | tRNA (guanine) methyltransferase activity | 6 | 1 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 1 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 277 | 281 | PF00656 | 0.471 |
CLV_C14_Caspase3-7 | 514 | 518 | PF00656 | 0.563 |
CLV_C14_Caspase3-7 | 559 | 563 | PF00656 | 0.764 |
CLV_C14_Caspase3-7 | 572 | 576 | PF00656 | 0.562 |
CLV_MEL_PAP_1 | 466 | 472 | PF00089 | 0.429 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 379 | 381 | PF00675 | 0.216 |
CLV_NRD_NRD_1 | 476 | 478 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 481 | 483 | PF00675 | 0.350 |
CLV_NRD_NRD_1 | 529 | 531 | PF00675 | 0.547 |
CLV_NRD_NRD_1 | 566 | 568 | PF00675 | 0.630 |
CLV_PCSK_FUR_1 | 525 | 529 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.217 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.309 |
CLV_PCSK_KEX2_1 | 476 | 478 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 527 | 529 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 531 | 533 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 566 | 568 | PF00082 | 0.666 |
CLV_PCSK_PC1ET2_1 | 149 | 151 | PF00082 | 0.485 |
CLV_PCSK_PC1ET2_1 | 158 | 160 | PF00082 | 0.490 |
CLV_PCSK_PC1ET2_1 | 224 | 226 | PF00082 | 0.230 |
CLV_PCSK_PC1ET2_1 | 527 | 529 | PF00082 | 0.496 |
CLV_PCSK_PC1ET2_1 | 531 | 533 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 302 | 306 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 591 | 595 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.268 |
DEG_APCC_DBOX_1 | 468 | 476 | PF00400 | 0.361 |
DEG_APCC_DBOX_1 | 59 | 67 | PF00400 | 0.395 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.403 |
DEG_SCF_FBW7_1 | 486 | 493 | PF00400 | 0.353 |
DEG_SPOP_SBC_1 | 383 | 387 | PF00917 | 0.383 |
DOC_CDC14_PxL_1 | 80 | 88 | PF14671 | 0.410 |
DOC_CKS1_1 | 487 | 492 | PF01111 | 0.353 |
DOC_CKS1_1 | 548 | 553 | PF01111 | 0.709 |
DOC_CYCLIN_yCln2_LP_2 | 28 | 34 | PF00134 | 0.447 |
DOC_MAPK_gen_1 | 473 | 481 | PF00069 | 0.442 |
DOC_MAPK_gen_1 | 500 | 508 | PF00069 | 0.424 |
DOC_MAPK_MEF2A_6 | 501 | 510 | PF00069 | 0.495 |
DOC_MAPK_RevD_3 | 470 | 483 | PF00069 | 0.409 |
DOC_PP2B_LxvP_1 | 28 | 31 | PF13499 | 0.450 |
DOC_PP2B_LxvP_1 | 335 | 338 | PF13499 | 0.428 |
DOC_PP4_FxxP_1 | 16 | 19 | PF00568 | 0.358 |
DOC_PP4_FxxP_1 | 441 | 444 | PF00568 | 0.344 |
DOC_PP4_FxxP_1 | 54 | 57 | PF00568 | 0.439 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 242 | 246 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 542 | 546 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.405 |
DOC_USP7_UBL2_3 | 527 | 531 | PF12436 | 0.488 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.416 |
DOC_WW_Pin1_4 | 486 | 491 | PF00397 | 0.417 |
DOC_WW_Pin1_4 | 499 | 504 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.373 |
DOC_WW_Pin1_4 | 544 | 549 | PF00397 | 0.610 |
LIG_14-3-3_CanoR_1 | 29 | 35 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 342 | 352 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 469 | 473 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 74 | 80 | PF00244 | 0.352 |
LIG_Actin_WH2_2 | 459 | 475 | PF00022 | 0.340 |
LIG_Actin_WH2_2 | 59 | 76 | PF00022 | 0.343 |
LIG_AP2alpha_2 | 255 | 257 | PF02296 | 0.415 |
LIG_BIR_III_4 | 278 | 282 | PF00653 | 0.446 |
LIG_CSL_BTD_1 | 441 | 444 | PF09270 | 0.432 |
LIG_deltaCOP1_diTrp_1 | 47 | 54 | PF00928 | 0.446 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.579 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.433 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.374 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.353 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.428 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.453 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.540 |
LIG_FHA_1 | 416 | 422 | PF00498 | 0.383 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.417 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.429 |
LIG_FHA_2 | 315 | 321 | PF00498 | 0.444 |
LIG_FHA_2 | 448 | 454 | PF00498 | 0.392 |
LIG_FHA_2 | 551 | 557 | PF00498 | 0.637 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.427 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.407 |
LIG_LIR_Apic_2 | 15 | 19 | PF02991 | 0.393 |
LIG_LIR_Apic_2 | 165 | 171 | PF02991 | 0.519 |
LIG_LIR_Apic_2 | 440 | 444 | PF02991 | 0.375 |
LIG_LIR_Apic_2 | 52 | 57 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 20 | 28 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 431 | 439 | PF02991 | 0.323 |
LIG_LIR_Gen_1 | 48 | 58 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 87 | 94 | PF02991 | 0.464 |
LIG_LIR_LC3C_4 | 431 | 435 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 20 | 24 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 328 | 333 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 412 | 416 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 431 | 435 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 47 | 53 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 520 | 524 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 87 | 93 | PF02991 | 0.459 |
LIG_Pex14_1 | 50 | 54 | PF04695 | 0.417 |
LIG_SH2_CRK | 333 | 337 | PF00017 | 0.509 |
LIG_SH2_PTP2 | 176 | 179 | PF00017 | 0.362 |
LIG_SH2_PTP2 | 3 | 6 | PF00017 | 0.338 |
LIG_SH2_STAP1 | 133 | 137 | PF00017 | 0.389 |
LIG_SH2_STAP1 | 144 | 148 | PF00017 | 0.316 |
LIG_SH2_STAT3 | 133 | 136 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 3 | 6 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 432 | 435 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 449 | 452 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.350 |
LIG_SH3_3 | 250 | 256 | PF00018 | 0.444 |
LIG_SH3_3 | 385 | 391 | PF00018 | 0.655 |
LIG_SH3_3 | 452 | 458 | PF00018 | 0.351 |
LIG_SH3_3 | 484 | 490 | PF00018 | 0.481 |
LIG_SH3_3 | 545 | 551 | PF00018 | 0.592 |
LIG_TRAF2_1 | 234 | 237 | PF00917 | 0.509 |
LIG_TRAF2_1 | 317 | 320 | PF00917 | 0.471 |
LIG_TRFH_1 | 333 | 337 | PF08558 | 0.446 |
LIG_UBA3_1 | 478 | 483 | PF00899 | 0.357 |
MOD_CDK_SPxxK_3 | 53 | 60 | PF00069 | 0.384 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.604 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.512 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.398 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.391 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.513 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.485 |
MOD_CK1_1 | 546 | 552 | PF00069 | 0.679 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.444 |
MOD_CK1_1 | 598 | 604 | PF00069 | 0.421 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.451 |
MOD_CK2_1 | 314 | 320 | PF00069 | 0.450 |
MOD_CK2_1 | 447 | 453 | PF00069 | 0.404 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.433 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.457 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.205 |
MOD_Cter_Amidation | 140 | 143 | PF01082 | 0.435 |
MOD_Cter_Amidation | 567 | 570 | PF01082 | 0.716 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.621 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.457 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.399 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.269 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.277 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.364 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.498 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.553 |
MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.681 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.374 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.642 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.359 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.676 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.378 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.377 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.423 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.606 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.562 |
MOD_GSK3_1 | 546 | 553 | PF00069 | 0.634 |
MOD_GSK3_1 | 604 | 611 | PF00069 | 0.665 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.463 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.551 |
MOD_N-GLC_1 | 242 | 247 | PF02516 | 0.309 |
MOD_N-GLC_1 | 343 | 348 | PF02516 | 0.271 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.534 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.427 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.471 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.355 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.428 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.393 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.407 |
MOD_NEK2_2 | 75 | 80 | PF00069 | 0.346 |
MOD_PKA_1 | 142 | 148 | PF00069 | 0.437 |
MOD_PKA_1 | 569 | 575 | PF00069 | 0.616 |
MOD_PKA_2 | 468 | 474 | PF00069 | 0.364 |
MOD_PKA_2 | 493 | 499 | PF00069 | 0.511 |
MOD_PKB_1 | 567 | 575 | PF00069 | 0.678 |
MOD_Plk_1 | 123 | 129 | PF00069 | 0.478 |
MOD_Plk_1 | 235 | 241 | PF00069 | 0.471 |
MOD_Plk_1 | 343 | 349 | PF00069 | 0.471 |
MOD_Plk_2-3 | 447 | 453 | PF00069 | 0.492 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.471 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.429 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.391 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.509 |
MOD_Plk_4 | 428 | 434 | PF00069 | 0.351 |
MOD_Plk_4 | 437 | 443 | PF00069 | 0.329 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.492 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.468 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.671 |
MOD_ProDKin_1 | 291 | 297 | PF00069 | 0.509 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.421 |
MOD_ProDKin_1 | 486 | 492 | PF00069 | 0.412 |
MOD_ProDKin_1 | 499 | 505 | PF00069 | 0.631 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.377 |
MOD_ProDKin_1 | 544 | 550 | PF00069 | 0.614 |
MOD_SUMO_for_1 | 526 | 529 | PF00179 | 0.590 |
MOD_SUMO_rev_2 | 145 | 151 | PF00179 | 0.492 |
MOD_SUMO_rev_2 | 56 | 66 | PF00179 | 0.346 |
TRG_DiLeu_BaEn_1 | 68 | 73 | PF01217 | 0.410 |
TRG_DiLeu_BaEn_4 | 318 | 324 | PF01217 | 0.495 |
TRG_DiLeu_BaLyEn_6 | 195 | 200 | PF01217 | 0.456 |
TRG_DiLeu_BaLyEn_6 | 474 | 479 | PF01217 | 0.387 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 3 | 6 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 432 | 435 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.350 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.408 |
TRG_ER_diArg_1 | 222 | 225 | PF00400 | 0.407 |
TRG_ER_diArg_1 | 301 | 303 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 340 | 343 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 475 | 477 | PF00400 | 0.325 |
TRG_ER_diArg_1 | 566 | 569 | PF00400 | 0.666 |
TRG_Pf-PMV_PEXEL_1 | 507 | 511 | PF00026 | 0.486 |
TRG_Pf-PMV_PEXEL_1 | 64 | 68 | PF00026 | 0.443 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAW4 | Leptomonas seymouri | 68% | 100% |
A0A0S4JG90 | Bodo saltans | 36% | 100% |
A0A1X0NLX9 | Trypanosomatidae | 43% | 100% |
A0A3S7WP82 | Leishmania donovani | 92% | 100% |
A0A422N510 | Trypanosoma rangeli | 45% | 100% |
A4H4E6 | Leishmania braziliensis | 86% | 100% |
A4HSM3 | Leishmania infantum | 92% | 100% |
Q12463 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 27% | 100% |
Q4QJA1 | Leishmania major | 92% | 100% |
Q54QA6 | Dictyostelium discoideum | 27% | 100% |
Q9CWH5 | Mus musculus | 28% | 100% |
V5B7D5 | Trypanosoma cruzi | 45% | 100% |