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. | yes | yes: 5 |
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: 16 |
NetGPI | no | yes: 0, no: 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005739 | mitochondrion | 5 | 12 |
GO:0043226 | organelle | 2 | 16 |
GO:0043227 | membrane-bounded organelle | 3 | 16 |
GO:0043229 | intracellular organelle | 3 | 16 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 16 |
GO:0110165 | cellular anatomical entity | 1 | 16 |
Related structures:
AlphaFold database: A4HNH1
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 16 |
GO:0006396 | RNA processing | 6 | 16 |
GO:0006399 | tRNA metabolic process | 7 | 16 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 16 |
GO:0006807 | nitrogen compound metabolic process | 2 | 16 |
GO:0008033 | tRNA processing | 8 | 16 |
GO:0008152 | metabolic process | 1 | 16 |
GO:0009987 | cellular process | 1 | 16 |
GO:0016070 | RNA metabolic process | 5 | 16 |
GO:0034470 | ncRNA processing | 7 | 16 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 16 |
GO:0034660 | ncRNA metabolic process | 6 | 16 |
GO:0043170 | macromolecule metabolic process | 3 | 16 |
GO:0044237 | cellular metabolic process | 2 | 16 |
GO:0044238 | primary metabolic process | 2 | 16 |
GO:0046483 | heterocycle metabolic process | 3 | 16 |
GO:0071704 | organic substance metabolic process | 2 | 16 |
GO:0090304 | nucleic acid metabolic process | 4 | 16 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 16 |
GO:0000966 | RNA 5'-end processing | 7 | 1 |
GO:0001682 | tRNA 5'-leader removal | 9 | 1 |
GO:0099116 | tRNA 5'-end processing | 8 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 16 |
GO:0016787 | hydrolase activity | 2 | 16 |
GO:0004518 | nuclease activity | 4 | 6 |
GO:0004519 | endonuclease activity | 5 | 5 |
GO:0004521 | RNA endonuclease activity | 5 | 5 |
GO:0004526 | ribonuclease P activity | 6 | 5 |
GO:0004540 | RNA nuclease activity | 4 | 5 |
GO:0004549 | tRNA-specific ribonuclease activity | 5 | 5 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 6 |
GO:0016891 | RNA endonuclease activity, producing 5'-phosphomonoesters | 6 | 5 |
GO:0016893 | endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 5 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 5 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 5 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 347 | 351 | PF00656 | 0.476 |
CLV_C14_Caspase3-7 | 365 | 369 | PF00656 | 0.494 |
CLV_C14_Caspase3-7 | 464 | 468 | PF00656 | 0.450 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.300 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.377 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.677 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.331 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.396 |
CLV_PCSK_PC1ET2_1 | 15 | 17 | PF00082 | 0.768 |
CLV_PCSK_PC1ET2_1 | 173 | 175 | PF00082 | 0.408 |
CLV_PCSK_PC7_1 | 47 | 53 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.272 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 487 | 491 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.466 |
CLV_Separin_Metazoa | 92 | 96 | PF03568 | 0.518 |
DEG_APCC_DBOX_1 | 160 | 168 | PF00400 | 0.354 |
DOC_CKS1_1 | 106 | 111 | PF01111 | 0.368 |
DOC_CKS1_1 | 427 | 432 | PF01111 | 0.260 |
DOC_CYCLIN_RxL_1 | 257 | 266 | PF00134 | 0.488 |
DOC_MAPK_DCC_7 | 386 | 395 | PF00069 | 0.566 |
DOC_MAPK_gen_1 | 173 | 182 | PF00069 | 0.423 |
DOC_MAPK_gen_1 | 411 | 420 | PF00069 | 0.304 |
DOC_MAPK_gen_1 | 506 | 515 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 140 | 148 | PF00069 | 0.342 |
DOC_MAPK_MEF2A_6 | 509 | 517 | PF00069 | 0.459 |
DOC_MAPK_MEF2A_6 | 75 | 82 | PF00069 | 0.531 |
DOC_PP4_FxxP_1 | 387 | 390 | PF00568 | 0.591 |
DOC_SPAK_OSR1_1 | 386 | 390 | PF12202 | 0.587 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.339 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.375 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.256 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.297 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.292 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 265 | 270 | PF00397 | 0.497 |
DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.353 |
DOC_WW_Pin1_4 | 445 | 450 | PF00397 | 0.366 |
LIG_14-3-3_CanoR_1 | 236 | 240 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 495 | 501 | PF00244 | 0.375 |
LIG_14-3-3_CanoR_1 | 509 | 514 | PF00244 | 0.330 |
LIG_14-3-3_CanoR_1 | 519 | 524 | PF00244 | 0.317 |
LIG_14-3-3_CterR_2 | 579 | 581 | PF00244 | 0.380 |
LIG_Actin_WH2_2 | 134 | 149 | PF00022 | 0.445 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.664 |
LIG_BIR_III_2 | 165 | 169 | PF00653 | 0.481 |
LIG_BIR_III_2 | 20 | 24 | PF00653 | 0.421 |
LIG_BIR_III_4 | 63 | 67 | PF00653 | 0.384 |
LIG_BRCT_BRCA1_1 | 190 | 194 | PF00533 | 0.381 |
LIG_BRCT_BRCA1_1 | 383 | 387 | PF00533 | 0.651 |
LIG_BRCT_BRCA1_1 | 447 | 451 | PF00533 | 0.409 |
LIG_Clathr_ClatBox_1 | 37 | 41 | PF01394 | 0.321 |
LIG_CtBP_PxDLS_1 | 22 | 26 | PF00389 | 0.380 |
LIG_deltaCOP1_diTrp_1 | 573 | 578 | PF00928 | 0.401 |
LIG_EVH1_1 | 446 | 450 | PF00568 | 0.220 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.571 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.407 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.509 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.350 |
LIG_FHA_1 | 570 | 576 | PF00498 | 0.493 |
LIG_FHA_2 | 227 | 233 | PF00498 | 0.398 |
LIG_FHA_2 | 345 | 351 | PF00498 | 0.405 |
LIG_FHA_2 | 462 | 468 | PF00498 | 0.359 |
LIG_GBD_Chelix_1 | 296 | 304 | PF00786 | 0.385 |
LIG_LIR_Apic_2 | 384 | 390 | PF02991 | 0.595 |
LIG_LIR_Gen_1 | 191 | 200 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 332 | 340 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 342 | 352 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 454 | 463 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 191 | 197 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 209 | 215 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 332 | 336 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 342 | 348 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 454 | 459 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 478 | 484 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 499 | 503 | PF02991 | 0.352 |
LIG_MAD2 | 101 | 109 | PF02301 | 0.354 |
LIG_Pex14_1 | 208 | 212 | PF04695 | 0.361 |
LIG_Pex14_1 | 536 | 540 | PF04695 | 0.452 |
LIG_Pex14_2 | 133 | 137 | PF04695 | 0.510 |
LIG_Pex14_2 | 177 | 181 | PF04695 | 0.344 |
LIG_Pex14_2 | 387 | 391 | PF04695 | 0.615 |
LIG_Pex14_2 | 488 | 492 | PF04695 | 0.350 |
LIG_PTB_Apo_2 | 175 | 182 | PF02174 | 0.252 |
LIG_PTB_Apo_2 | 450 | 457 | PF02174 | 0.338 |
LIG_PTB_Apo_2 | 56 | 63 | PF02174 | 0.374 |
LIG_PTB_Phospho_1 | 450 | 456 | PF10480 | 0.338 |
LIG_REV1ctd_RIR_1 | 486 | 495 | PF16727 | 0.350 |
LIG_SH2_CRK | 345 | 349 | PF00017 | 0.397 |
LIG_SH2_CRK | 460 | 464 | PF00017 | 0.348 |
LIG_SH2_SRC | 363 | 366 | PF00017 | 0.344 |
LIG_SH2_STAP1 | 345 | 349 | PF00017 | 0.377 |
LIG_SH2_STAP1 | 435 | 439 | PF00017 | 0.293 |
LIG_SH2_STAP1 | 521 | 525 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 480 | 483 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 516 | 519 | PF00017 | 0.226 |
LIG_SH2_STAT5 | 540 | 543 | PF00017 | 0.459 |
LIG_SH3_1 | 16 | 22 | PF00018 | 0.516 |
LIG_SH3_3 | 16 | 22 | PF00018 | 0.513 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.458 |
LIG_SH3_3 | 386 | 392 | PF00018 | 0.457 |
LIG_SH3_3 | 444 | 450 | PF00018 | 0.220 |
LIG_SH3_3 | 480 | 486 | PF00018 | 0.505 |
LIG_SH3_4 | 306 | 313 | PF00018 | 0.431 |
LIG_SUMO_SIM_anti_2 | 416 | 421 | PF11976 | 0.220 |
LIG_SUMO_SIM_anti_2 | 542 | 548 | PF11976 | 0.537 |
LIG_SUMO_SIM_par_1 | 36 | 41 | PF11976 | 0.321 |
LIG_TRFH_1 | 286 | 290 | PF08558 | 0.361 |
LIG_TYR_ITIM | 354 | 359 | PF00017 | 0.378 |
LIG_WRC_WIRS_1 | 283 | 288 | PF05994 | 0.423 |
MOD_CDC14_SPxK_1 | 4 | 7 | PF00782 | 0.533 |
MOD_CDK_SPxK_1 | 1 | 7 | PF00069 | 0.535 |
MOD_CDK_SPxxK_3 | 286 | 293 | PF00069 | 0.361 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.434 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.578 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.625 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.354 |
MOD_CK2_1 | 226 | 232 | PF00069 | 0.409 |
MOD_CK2_1 | 28 | 34 | PF00069 | 0.395 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.502 |
MOD_CK2_1 | 397 | 403 | PF00069 | 0.456 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.529 |
MOD_Cter_Amidation | 412 | 415 | PF01082 | 0.350 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.497 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.571 |
MOD_GlcNHglycan | 24 | 28 | PF01048 | 0.572 |
MOD_GlcNHglycan | 441 | 445 | PF01048 | 0.306 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.586 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.439 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.561 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.660 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.372 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.250 |
MOD_GSK3_1 | 553 | 560 | PF00069 | 0.621 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.391 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.382 |
MOD_N-GLC_1 | 124 | 129 | PF02516 | 0.291 |
MOD_N-GLC_1 | 431 | 436 | PF02516 | 0.360 |
MOD_N-GLC_1 | 504 | 509 | PF02516 | 0.440 |
MOD_N-GLC_1 | 551 | 556 | PF02516 | 0.693 |
MOD_N-GLC_1 | 557 | 562 | PF02516 | 0.691 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.507 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.387 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.560 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.500 |
MOD_PIKK_1 | 529 | 535 | PF00454 | 0.491 |
MOD_PK_1 | 519 | 525 | PF00069 | 0.375 |
MOD_PKA_2 | 235 | 241 | PF00069 | 0.292 |
MOD_PKA_2 | 496 | 502 | PF00069 | 0.399 |
MOD_PKA_2 | 508 | 514 | PF00069 | 0.357 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.342 |
MOD_PKB_1 | 438 | 446 | PF00069 | 0.220 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.287 |
MOD_Plk_1 | 234 | 240 | PF00069 | 0.443 |
MOD_Plk_1 | 27 | 33 | PF00069 | 0.348 |
MOD_Plk_1 | 431 | 437 | PF00069 | 0.429 |
MOD_Plk_1 | 440 | 446 | PF00069 | 0.326 |
MOD_Plk_1 | 551 | 557 | PF00069 | 0.721 |
MOD_Plk_2-3 | 28 | 34 | PF00069 | 0.484 |
MOD_Plk_2-3 | 341 | 347 | PF00069 | 0.399 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.476 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.520 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.375 |
MOD_Plk_4 | 344 | 350 | PF00069 | 0.434 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.374 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.424 |
MOD_Plk_4 | 413 | 419 | PF00069 | 0.355 |
MOD_Plk_4 | 519 | 525 | PF00069 | 0.343 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.377 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.298 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.535 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.478 |
MOD_ProDKin_1 | 265 | 271 | PF00069 | 0.497 |
MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.626 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.353 |
MOD_ProDKin_1 | 445 | 451 | PF00069 | 0.366 |
MOD_SUMO_rev_2 | 206 | 215 | PF00179 | 0.403 |
MOD_SUMO_rev_2 | 28 | 38 | PF00179 | 0.363 |
MOD_SUMO_rev_2 | 332 | 339 | PF00179 | 0.440 |
MOD_SUMO_rev_2 | 360 | 369 | PF00179 | 0.445 |
TRG_DiLeu_BaEn_1 | 235 | 240 | PF01217 | 0.385 |
TRG_DiLeu_BaEn_1 | 34 | 39 | PF01217 | 0.539 |
TRG_ENDOCYTIC_2 | 212 | 215 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 345 | 348 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 356 | 359 | PF00928 | 0.384 |
TRG_ENDOCYTIC_2 | 456 | 459 | PF00928 | 0.346 |
TRG_ENDOCYTIC_2 | 460 | 463 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 480 | 483 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 500 | 503 | PF00928 | 0.197 |
TRG_ER_diArg_1 | 16 | 19 | PF00400 | 0.626 |
TRG_ER_diArg_1 | 160 | 162 | PF00400 | 0.435 |
TRG_ER_diArg_1 | 174 | 176 | PF00400 | 0.348 |
TRG_ER_diArg_1 | 371 | 374 | PF00400 | 0.503 |
TRG_ER_diArg_1 | 492 | 495 | PF00400 | 0.326 |
TRG_NLS_Bipartite_1 | 161 | 177 | PF00514 | 0.518 |
TRG_NLS_MonoCore_2 | 14 | 19 | PF00514 | 0.620 |
TRG_NLS_MonoExtC_3 | 14 | 19 | PF00514 | 0.759 |
TRG_NLS_MonoExtN_4 | 12 | 19 | PF00514 | 0.765 |
TRG_Pf-PMV_PEXEL_1 | 161 | 165 | PF00026 | 0.500 |
TRG_Pf-PMV_PEXEL_1 | 423 | 427 | PF00026 | 0.260 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I198 | Leptomonas seymouri | 65% | 98% |
A0A0S4JLM5 | Bodo saltans | 39% | 100% |
A0A1X0P3X4 | Trypanosomatidae | 32% | 100% |
A0A1X0P680 | Trypanosomatidae | 41% | 100% |
A0A3Q8IIJ5 | Leishmania donovani | 80% | 99% |
A0A3R7LTW4 | Trypanosoma rangeli | 45% | 100% |
A0A422MWI6 | Trypanosoma rangeli | 31% | 100% |
A4HLQ7 | Leishmania braziliensis | 30% | 82% |
A4IC62 | Leishmania infantum | 81% | 99% |
C9ZYE1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
D0A6B5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9AFY2 | Leishmania major | 82% | 100% |
E9B735 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 99% |
V5B8T9 | Trypanosoma cruzi | 44% | 100% |
V5BPA7 | Trypanosoma cruzi | 29% | 100% |