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: A4H4E6
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 | 293 | 297 | PF00656 | 0.472 |
CLV_C14_Caspase3-7 | 405 | 409 | PF00656 | 0.471 |
CLV_C14_Caspase3-7 | 521 | 525 | PF00656 | 0.566 |
CLV_MEL_PAP_1 | 473 | 479 | PF00089 | 0.436 |
CLV_NRD_NRD_1 | 238 | 240 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 317 | 319 | PF00675 | 0.310 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.217 |
CLV_NRD_NRD_1 | 483 | 485 | PF00675 | 0.333 |
CLV_NRD_NRD_1 | 488 | 490 | PF00675 | 0.355 |
CLV_NRD_NRD_1 | 536 | 538 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 574 | 576 | PF00675 | 0.629 |
CLV_PCSK_FUR_1 | 532 | 536 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 111 | 113 | PF00082 | 0.305 |
CLV_PCSK_KEX2_1 | 165 | 167 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.218 |
CLV_PCSK_KEX2_1 | 317 | 319 | PF00082 | 0.310 |
CLV_PCSK_KEX2_1 | 483 | 485 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 534 | 536 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 538 | 540 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 574 | 576 | PF00082 | 0.664 |
CLV_PCSK_KEX2_1 | 578 | 580 | PF00082 | 0.646 |
CLV_PCSK_PC1ET2_1 | 111 | 113 | PF00082 | 0.305 |
CLV_PCSK_PC1ET2_1 | 165 | 167 | PF00082 | 0.483 |
CLV_PCSK_PC1ET2_1 | 240 | 242 | PF00082 | 0.231 |
CLV_PCSK_PC1ET2_1 | 534 | 536 | PF00082 | 0.503 |
CLV_PCSK_PC1ET2_1 | 538 | 540 | PF00082 | 0.484 |
CLV_PCSK_PC1ET2_1 | 578 | 580 | PF00082 | 0.603 |
CLV_PCSK_PC7_1 | 574 | 580 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 318 | 322 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 599 | 603 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.269 |
DEG_APCC_DBOX_1 | 475 | 483 | PF00400 | 0.369 |
DEG_APCC_DBOX_1 | 75 | 83 | PF00400 | 0.393 |
DEG_SCF_FBW7_1 | 493 | 500 | PF00400 | 0.356 |
DEG_SPOP_SBC_1 | 549 | 553 | PF00917 | 0.434 |
DOC_CKS1_1 | 494 | 499 | PF01111 | 0.357 |
DOC_CYCLIN_yCln2_LP_2 | 44 | 50 | PF00134 | 0.448 |
DOC_MAPK_gen_1 | 480 | 488 | PF00069 | 0.449 |
DOC_MAPK_gen_1 | 507 | 515 | PF00069 | 0.430 |
DOC_MAPK_MEF2A_6 | 508 | 517 | PF00069 | 0.502 |
DOC_MAPK_RevD_3 | 477 | 490 | PF00069 | 0.416 |
DOC_PP1_RVXF_1 | 52 | 58 | PF00149 | 0.267 |
DOC_PP2B_LxvP_1 | 351 | 354 | PF13499 | 0.429 |
DOC_PP2B_LxvP_1 | 44 | 47 | PF13499 | 0.449 |
DOC_PP4_FxxP_1 | 32 | 35 | PF00568 | 0.369 |
DOC_PP4_FxxP_1 | 448 | 451 | PF00568 | 0.346 |
DOC_PP4_FxxP_1 | 70 | 73 | PF00568 | 0.428 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 548 | 552 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 559 | 563 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.405 |
DOC_USP7_UBL2_3 | 534 | 538 | PF12436 | 0.493 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 307 | 312 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 493 | 498 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 506 | 511 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 553 | 558 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.369 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.474 |
LIG_14-3-3_CanoR_1 | 358 | 368 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 476 | 480 | PF00244 | 0.385 |
LIG_14-3-3_CanoR_1 | 90 | 96 | PF00244 | 0.362 |
LIG_Actin_WH2_2 | 466 | 482 | PF00022 | 0.346 |
LIG_Actin_WH2_2 | 75 | 92 | PF00022 | 0.343 |
LIG_AP2alpha_2 | 271 | 273 | PF02296 | 0.416 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.398 |
LIG_BIR_III_4 | 294 | 298 | PF00653 | 0.447 |
LIG_CSL_BTD_1 | 448 | 451 | PF09270 | 0.434 |
LIG_deltaCOP1_diTrp_1 | 334 | 346 | PF00928 | 0.358 |
LIG_deltaCOP1_diTrp_1 | 63 | 70 | PF00928 | 0.457 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.374 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.429 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.454 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.351 |
LIG_FHA_1 | 436 | 442 | PF00498 | 0.421 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.226 |
LIG_FHA_2 | 300 | 306 | PF00498 | 0.463 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.445 |
LIG_FHA_2 | 403 | 409 | PF00498 | 0.472 |
LIG_FHA_2 | 455 | 461 | PF00498 | 0.399 |
LIG_FHA_2 | 558 | 564 | PF00498 | 0.633 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.441 |
LIG_FHA_2 | 99 | 105 | PF00498 | 0.413 |
LIG_LIR_Apic_2 | 181 | 187 | PF02991 | 0.517 |
LIG_LIR_Apic_2 | 30 | 35 | PF02991 | 0.399 |
LIG_LIR_Apic_2 | 447 | 451 | PF02991 | 0.378 |
LIG_LIR_Apic_2 | 68 | 73 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 103 | 110 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 36 | 44 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 64 | 74 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 103 | 109 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 188 | 194 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 344 | 349 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 36 | 40 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 419 | 423 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 526 | 531 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 63 | 69 | PF02991 | 0.374 |
LIG_PCNA_yPIPBox_3 | 207 | 219 | PF02747 | 0.468 |
LIG_PDZ_Class_1 | 616 | 621 | PF00595 | 0.479 |
LIG_Pex14_1 | 66 | 70 | PF04695 | 0.426 |
LIG_SH2_CRK | 349 | 353 | PF00017 | 0.510 |
LIG_SH2_PTP2 | 19 | 22 | PF00017 | 0.346 |
LIG_SH2_PTP2 | 192 | 195 | PF00017 | 0.361 |
LIG_SH2_STAP1 | 149 | 153 | PF00017 | 0.392 |
LIG_SH2_STAP1 | 160 | 164 | PF00017 | 0.313 |
LIG_SH2_STAT3 | 149 | 152 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 192 | 195 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.365 |
LIG_SH3_3 | 266 | 272 | PF00018 | 0.445 |
LIG_SH3_3 | 459 | 465 | PF00018 | 0.357 |
LIG_SH3_3 | 491 | 497 | PF00018 | 0.481 |
LIG_TRAF2_1 | 250 | 253 | PF00917 | 0.510 |
LIG_TRAF2_1 | 323 | 326 | PF00917 | 0.358 |
LIG_TRAF2_1 | 333 | 336 | PF00917 | 0.472 |
LIG_TRFH_1 | 349 | 353 | PF08558 | 0.447 |
LIG_UBA3_1 | 485 | 490 | PF00899 | 0.362 |
LIG_WRC_WIRS_1 | 417 | 422 | PF05994 | 0.346 |
MOD_CDK_SPxxK_3 | 69 | 76 | PF00069 | 0.380 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.576 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.505 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.398 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.456 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.392 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.514 |
MOD_CK1_1 | 463 | 469 | PF00069 | 0.403 |
MOD_CK1_1 | 500 | 506 | PF00069 | 0.489 |
MOD_CK1_1 | 551 | 557 | PF00069 | 0.637 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.369 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.439 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.358 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.451 |
MOD_CK2_1 | 454 | 460 | PF00069 | 0.409 |
MOD_CK2_1 | 557 | 563 | PF00069 | 0.590 |
MOD_CK2_1 | 65 | 71 | PF00069 | 0.440 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.451 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.217 |
MOD_Cter_Amidation | 156 | 159 | PF01082 | 0.441 |
MOD_Cter_Amidation | 575 | 578 | PF01082 | 0.708 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.544 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.454 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.399 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.380 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.270 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.278 |
MOD_GlcNHglycan | 376 | 379 | PF01048 | 0.365 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.489 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.397 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.412 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.540 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.618 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.388 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.280 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.686 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.437 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.379 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.608 |
MOD_GSK3_1 | 548 | 555 | PF00069 | 0.572 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.433 |
MOD_GSK3_1 | 612 | 619 | PF00069 | 0.677 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.475 |
MOD_N-GLC_1 | 258 | 263 | PF02516 | 0.310 |
MOD_N-GLC_1 | 359 | 364 | PF02516 | 0.272 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.532 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.398 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.428 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.472 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.357 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.439 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.422 |
MOD_NEK2_2 | 91 | 96 | PF00069 | 0.357 |
MOD_PKA_1 | 158 | 164 | PF00069 | 0.439 |
MOD_PKA_2 | 475 | 481 | PF00069 | 0.373 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.397 |
MOD_PKA_2 | 500 | 506 | PF00069 | 0.515 |
MOD_Plk_1 | 139 | 145 | PF00069 | 0.502 |
MOD_Plk_1 | 251 | 257 | PF00069 | 0.472 |
MOD_Plk_1 | 359 | 365 | PF00069 | 0.472 |
MOD_Plk_2-3 | 454 | 460 | PF00069 | 0.497 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.472 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.430 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.392 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.510 |
MOD_Plk_4 | 444 | 450 | PF00069 | 0.334 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.501 |
MOD_Plk_4 | 91 | 97 | PF00069 | 0.481 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.644 |
MOD_ProDKin_1 | 307 | 313 | PF00069 | 0.510 |
MOD_ProDKin_1 | 493 | 499 | PF00069 | 0.414 |
MOD_ProDKin_1 | 506 | 512 | PF00069 | 0.635 |
MOD_ProDKin_1 | 553 | 559 | PF00069 | 0.622 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.373 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.474 |
MOD_SUMO_for_1 | 533 | 536 | PF00179 | 0.596 |
MOD_SUMO_rev_2 | 161 | 167 | PF00179 | 0.489 |
MOD_SUMO_rev_2 | 597 | 604 | PF00179 | 0.398 |
TRG_DiLeu_BaEn_1 | 84 | 89 | PF01217 | 0.412 |
TRG_DiLeu_BaEn_3 | 252 | 258 | PF01217 | 0.453 |
TRG_DiLeu_BaLyEn_6 | 211 | 216 | PF01217 | 0.463 |
TRG_DiLeu_BaLyEn_6 | 481 | 486 | PF01217 | 0.393 |
TRG_ENDOCYTIC_2 | 106 | 109 | PF00928 | 0.419 |
TRG_ENDOCYTIC_2 | 19 | 22 | PF00928 | 0.346 |
TRG_ENDOCYTIC_2 | 191 | 194 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 270 | 273 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 93 | 96 | PF00928 | 0.365 |
TRG_ER_diArg_1 | 238 | 241 | PF00400 | 0.410 |
TRG_ER_diArg_1 | 317 | 319 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 356 | 359 | PF00400 | 0.429 |
TRG_ER_diArg_1 | 482 | 484 | PF00400 | 0.331 |
TRG_ER_diArg_1 | 574 | 577 | PF00400 | 0.661 |
TRG_NLS_MonoExtN_4 | 574 | 581 | PF00514 | 0.590 |
TRG_Pf-PMV_PEXEL_1 | 514 | 518 | PF00026 | 0.489 |
TRG_Pf-PMV_PEXEL_1 | 80 | 84 | PF00026 | 0.442 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAW4 | Leptomonas seymouri | 67% | 100% |
A0A0S4JG90 | Bodo saltans | 36% | 100% |
A0A1X0NLX9 | Trypanosomatidae | 43% | 100% |
A0A3S7WP82 | Leishmania donovani | 85% | 100% |
A0A422N510 | Trypanosoma rangeli | 42% | 100% |
A4HSM3 | Leishmania infantum | 85% | 100% |
E9AKK7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q05B63 | Bos taurus | 27% | 100% |
Q12463 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
Q4QJA1 | Leishmania major | 84% | 100% |
Q54QA6 | Dictyostelium discoideum | 26% | 100% |
Q5R962 | Pongo abelii | 27% | 100% |
Q6NS23 | Xenopus laevis | 26% | 100% |
Q7TNK6 | Rattus norvegicus | 28% | 100% |
Q7Z4G4 | Homo sapiens | 28% | 100% |
Q9CWH5 | Mus musculus | 27% | 100% |
V5B7D5 | Trypanosoma cruzi | 44% | 100% |