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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 9 |
GO:0006396 | RNA processing | 6 | 9 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016070 | RNA metabolic process | 5 | 9 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0046483 | heterocycle metabolic process | 3 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:0090304 | nucleic acid metabolic process | 4 | 9 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 9 |
GO:0032259 | methylation | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 9 |
GO:0003723 | RNA binding | 4 | 9 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0005488 | binding | 1 | 9 |
GO:0008168 | methyltransferase activity | 4 | 10 |
GO:0008173 | RNA methyltransferase activity | 4 | 9 |
GO:0016740 | transferase activity | 2 | 10 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 9 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 392 | 394 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.466 |
CLV_NRD_NRD_1 | 492 | 494 | PF00675 | 0.481 |
CLV_NRD_NRD_1 | 506 | 508 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 513 | 515 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 518 | 520 | PF00675 | 0.430 |
CLV_PCSK_FUR_1 | 485 | 489 | PF00082 | 0.419 |
CLV_PCSK_FUR_1 | 516 | 520 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 487 | 489 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 506 | 508 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 513 | 515 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 518 | 520 | PF00082 | 0.432 |
CLV_PCSK_PC1ET2_1 | 379 | 381 | PF00082 | 0.420 |
CLV_PCSK_PC7_1 | 380 | 386 | PF00082 | 0.424 |
CLV_PCSK_PC7_1 | 388 | 394 | PF00082 | 0.425 |
CLV_PCSK_PC7_1 | 487 | 493 | PF00082 | 0.530 |
CLV_PCSK_PC7_1 | 514 | 520 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 527 | 531 | PF00082 | 0.719 |
CLV_PCSK_SKI1_1 | 551 | 555 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.400 |
DEG_APCC_DBOX_1 | 266 | 274 | PF00400 | 0.359 |
DEG_APCC_DBOX_1 | 379 | 387 | PF00400 | 0.600 |
DEG_APCC_DBOX_1 | 395 | 403 | PF00400 | 0.407 |
DEG_ODPH_VHL_1 | 19 | 31 | PF01847 | 0.475 |
DEG_SPOP_SBC_1 | 42 | 46 | PF00917 | 0.636 |
DOC_CKS1_1 | 171 | 176 | PF01111 | 0.508 |
DOC_CYCLIN_RxL_1 | 184 | 197 | PF00134 | 0.398 |
DOC_MAPK_gen_1 | 142 | 150 | PF00069 | 0.401 |
DOC_MAPK_gen_1 | 392 | 399 | PF00069 | 0.467 |
DOC_MAPK_gen_1 | 516 | 526 | PF00069 | 0.479 |
DOC_MAPK_gen_1 | 57 | 65 | PF00069 | 0.385 |
DOC_MAPK_gen_1 | 98 | 107 | PF00069 | 0.358 |
DOC_MAPK_JIP1_4 | 123 | 129 | PF00069 | 0.483 |
DOC_MAPK_MEF2A_6 | 448 | 456 | PF00069 | 0.532 |
DOC_PP1_RVXF_1 | 69 | 75 | PF00149 | 0.341 |
DOC_PP2B_LxvP_1 | 319 | 322 | PF13499 | 0.547 |
DOC_PP4_FxxP_1 | 169 | 172 | PF00568 | 0.367 |
DOC_PP4_FxxP_1 | 373 | 376 | PF00568 | 0.478 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.546 |
DOC_USP7_MATH_2 | 405 | 411 | PF00917 | 0.545 |
DOC_USP7_UBL2_3 | 58 | 62 | PF12436 | 0.374 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.712 |
DOC_WW_Pin1_4 | 401 | 406 | PF00397 | 0.548 |
LIG_14-3-3_CanoR_1 | 142 | 150 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 152 | 157 | PF00244 | 0.384 |
LIG_14-3-3_CanoR_1 | 308 | 312 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 323 | 329 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 392 | 399 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 458 | 464 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 546 | 550 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 9 | 19 | PF00244 | 0.650 |
LIG_Actin_WH2_2 | 79 | 94 | PF00022 | 0.299 |
LIG_BIR_III_4 | 280 | 284 | PF00653 | 0.402 |
LIG_CSL_BTD_1 | 522 | 525 | PF09270 | 0.691 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.427 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.553 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.656 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.392 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.522 |
LIG_FHA_2 | 246 | 252 | PF00498 | 0.532 |
LIG_FHA_2 | 434 | 440 | PF00498 | 0.617 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.397 |
LIG_LIR_Apic_2 | 13 | 18 | PF02991 | 0.635 |
LIG_LIR_Apic_2 | 168 | 172 | PF02991 | 0.363 |
LIG_LIR_Apic_2 | 561 | 567 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 368 | 376 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 255 | 261 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 368 | 373 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 430 | 434 | PF02991 | 0.483 |
LIG_NRBOX | 201 | 207 | PF00104 | 0.446 |
LIG_NRP_CendR_1 | 566 | 569 | PF00754 | 0.581 |
LIG_PCNA_yPIPBox_3 | 505 | 519 | PF02747 | 0.557 |
LIG_RPA_C_Fungi | 502 | 514 | PF08784 | 0.453 |
LIG_SH2_CRK | 214 | 218 | PF00017 | 0.282 |
LIG_SH2_CRK | 258 | 262 | PF00017 | 0.358 |
LIG_SH2_CRK | 564 | 568 | PF00017 | 0.681 |
LIG_SH2_SRC | 431 | 434 | PF00017 | 0.563 |
LIG_SH2_STAP1 | 214 | 218 | PF00017 | 0.282 |
LIG_SH2_STAP1 | 227 | 231 | PF00017 | 0.282 |
LIG_SH2_STAP1 | 329 | 333 | PF00017 | 0.435 |
LIG_SH2_STAP1 | 497 | 501 | PF00017 | 0.427 |
LIG_SH2_STAT3 | 275 | 278 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 370 | 373 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 421 | 424 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.408 |
LIG_SH3_1 | 15 | 21 | PF00018 | 0.522 |
LIG_SH3_1 | 519 | 525 | PF00018 | 0.498 |
LIG_SH3_2 | 172 | 177 | PF14604 | 0.398 |
LIG_SH3_2 | 522 | 527 | PF14604 | 0.525 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.527 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.468 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.530 |
LIG_SH3_3 | 293 | 299 | PF00018 | 0.691 |
LIG_SH3_3 | 314 | 320 | PF00018 | 0.627 |
LIG_SH3_3 | 519 | 525 | PF00018 | 0.619 |
LIG_SH3_CIN85_PxpxPR_1 | 318 | 323 | PF14604 | 0.598 |
LIG_SUMO_SIM_anti_2 | 145 | 151 | PF11976 | 0.467 |
LIG_SUMO_SIM_par_1 | 145 | 151 | PF11976 | 0.387 |
LIG_SUMO_SIM_par_1 | 189 | 194 | PF11976 | 0.320 |
LIG_TRAF2_1 | 343 | 346 | PF00917 | 0.575 |
LIG_TRFH_1 | 421 | 425 | PF08558 | 0.415 |
LIG_UBA3_1 | 64 | 71 | PF00899 | 0.333 |
MOD_CDK_SPxxK_3 | 170 | 177 | PF00069 | 0.453 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.576 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.419 |
MOD_CK1_1 | 401 | 407 | PF00069 | 0.494 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.616 |
MOD_CK2_1 | 294 | 300 | PF00069 | 0.613 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.552 |
MOD_CK2_1 | 401 | 407 | PF00069 | 0.573 |
MOD_CK2_1 | 433 | 439 | PF00069 | 0.618 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.606 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.342 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.692 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.487 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.649 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.574 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.567 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.525 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.282 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.692 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.585 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.636 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.607 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.515 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.532 |
MOD_LATS_1 | 140 | 146 | PF00433 | 0.403 |
MOD_N-GLC_1 | 27 | 32 | PF02516 | 0.525 |
MOD_N-GLC_2 | 221 | 223 | PF02516 | 0.282 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.562 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.315 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.316 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.625 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.542 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.555 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.518 |
MOD_NEK2_2 | 245 | 250 | PF00069 | 0.391 |
MOD_PIKK_1 | 22 | 28 | PF00454 | 0.595 |
MOD_PIKK_1 | 288 | 294 | PF00454 | 0.533 |
MOD_PIKK_1 | 338 | 344 | PF00454 | 0.654 |
MOD_PK_1 | 152 | 158 | PF00069 | 0.468 |
MOD_PK_1 | 448 | 454 | PF00069 | 0.475 |
MOD_PKA_1 | 142 | 148 | PF00069 | 0.481 |
MOD_PKA_1 | 392 | 398 | PF00069 | 0.466 |
MOD_PKA_1 | 492 | 498 | PF00069 | 0.499 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.594 |
MOD_PKA_2 | 307 | 313 | PF00069 | 0.567 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.416 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.657 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.493 |
MOD_PKA_2 | 391 | 397 | PF00069 | 0.434 |
MOD_PKA_2 | 459 | 465 | PF00069 | 0.552 |
MOD_PKA_2 | 492 | 498 | PF00069 | 0.574 |
MOD_PKA_2 | 545 | 551 | PF00069 | 0.620 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.635 |
MOD_PKB_1 | 556 | 564 | PF00069 | 0.398 |
MOD_Plk_1 | 150 | 156 | PF00069 | 0.398 |
MOD_Plk_1 | 27 | 33 | PF00069 | 0.526 |
MOD_Plk_1 | 325 | 331 | PF00069 | 0.536 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.335 |
MOD_Plk_1 | 438 | 444 | PF00069 | 0.593 |
MOD_Plk_2-3 | 439 | 445 | PF00069 | 0.550 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.282 |
MOD_Plk_4 | 307 | 313 | PF00069 | 0.600 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.439 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.379 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.447 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.422 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.708 |
MOD_ProDKin_1 | 401 | 407 | PF00069 | 0.548 |
MOD_SUMO_for_1 | 249 | 252 | PF00179 | 0.412 |
TRG_DiLeu_BaEn_1 | 266 | 271 | PF01217 | 0.459 |
TRG_DiLeu_BaEn_2 | 478 | 484 | PF01217 | 0.384 |
TRG_DiLeu_BaLyEn_6 | 393 | 398 | PF01217 | 0.501 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.282 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 370 | 373 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 431 | 434 | PF00928 | 0.481 |
TRG_ER_diArg_1 | 383 | 385 | PF00400 | 0.433 |
TRG_ER_diArg_1 | 423 | 426 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 458 | 461 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 486 | 488 | PF00400 | 0.450 |
TRG_ER_diArg_1 | 491 | 493 | PF00400 | 0.467 |
TRG_ER_diArg_1 | 506 | 508 | PF00400 | 0.308 |
TRG_ER_diArg_1 | 512 | 514 | PF00400 | 0.439 |
TRG_ER_diArg_1 | 516 | 519 | PF00400 | 0.434 |
TRG_Pf-PMV_PEXEL_1 | 125 | 130 | PF00026 | 0.447 |
TRG_Pf-PMV_PEXEL_1 | 189 | 194 | PF00026 | 0.282 |
TRG_Pf-PMV_PEXEL_1 | 396 | 400 | PF00026 | 0.515 |
TRG_Pf-PMV_PEXEL_1 | 71 | 75 | PF00026 | 0.415 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEE8 | Leptomonas seymouri | 70% | 93% |
A0A1X0P5S3 | Trypanosomatidae | 50% | 98% |
A0A3S7X9F7 | Leishmania donovani | 94% | 94% |
A0A422P2S4 | Trypanosoma rangeli | 50% | 100% |
A4HMV6 | Leishmania braziliensis | 80% | 100% |
A4IBH7 | Leishmania infantum | 94% | 94% |
C9ZZ65 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 97% |
E9B6G8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 94% |