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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005794 | Golgi apparatus | 5 | 6 |
GO:0016020 | membrane | 2 | 5 |
GO:0043226 | organelle | 2 | 6 |
GO:0043227 | membrane-bounded organelle | 3 | 6 |
GO:0043229 | intracellular organelle | 3 | 6 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: A4HLV0
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 1 |
GO:0007030 | Golgi organization | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 137 | 141 | PF00656 | 0.385 |
CLV_C14_Caspase3-7 | 347 | 351 | PF00656 | 0.571 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.517 |
CLV_PCSK_KEX2_1 | 538 | 540 | PF00082 | 0.682 |
CLV_PCSK_PC1ET2_1 | 538 | 540 | PF00082 | 0.660 |
CLV_PCSK_SKI1_1 | 162 | 166 | PF00082 | 0.243 |
CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.385 |
DOC_CYCLIN_yCln2_LP_2 | 467 | 473 | PF00134 | 0.546 |
DOC_CYCLIN_yCln2_LP_2 | 526 | 532 | PF00134 | 0.656 |
DOC_MAPK_MEF2A_6 | 521 | 528 | PF00069 | 0.648 |
DOC_PP2B_LxvP_1 | 467 | 470 | PF13499 | 0.538 |
DOC_PP4_FxxP_1 | 498 | 501 | PF00568 | 0.515 |
DOC_PP4_MxPP_1 | 389 | 392 | PF00568 | 0.533 |
DOC_PP4_MxPP_1 | 522 | 525 | PF00568 | 0.643 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 462 | 466 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 476 | 480 | PF00917 | 0.587 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 304 | 309 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.764 |
DOC_WW_Pin1_4 | 359 | 364 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 425 | 430 | PF00397 | 0.752 |
DOC_WW_Pin1_4 | 469 | 474 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 537 | 542 | PF00397 | 0.565 |
LIG_14-3-3_CanoR_1 | 441 | 446 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 97 | 102 | PF00244 | 0.299 |
LIG_APCC_ABBA_1 | 63 | 68 | PF00400 | 0.402 |
LIG_BIR_III_2 | 140 | 144 | PF00653 | 0.385 |
LIG_BIR_III_2 | 491 | 495 | PF00653 | 0.555 |
LIG_BRCT_BRCA1_1 | 99 | 103 | PF00533 | 0.301 |
LIG_deltaCOP1_diTrp_1 | 196 | 204 | PF00928 | 0.385 |
LIG_EH_1 | 420 | 424 | PF12763 | 0.711 |
LIG_EH1_1 | 46 | 54 | PF00400 | 0.418 |
LIG_EVH1_1 | 330 | 334 | PF00568 | 0.554 |
LIG_EVH1_1 | 387 | 391 | PF00568 | 0.563 |
LIG_EVH1_1 | 498 | 502 | PF00568 | 0.529 |
LIG_EVH1_2 | 524 | 528 | PF00568 | 0.646 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.484 |
LIG_FHA_1 | 214 | 220 | PF00498 | 0.274 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.385 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.702 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.610 |
LIG_FHA_1 | 441 | 447 | PF00498 | 0.559 |
LIG_FHA_2 | 135 | 141 | PF00498 | 0.385 |
LIG_FHA_2 | 232 | 238 | PF00498 | 0.385 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.292 |
LIG_FHA_2 | 301 | 307 | PF00498 | 0.550 |
LIG_FHA_2 | 413 | 419 | PF00498 | 0.585 |
LIG_FHA_2 | 69 | 75 | PF00498 | 0.420 |
LIG_IRF3_LxIS_1 | 246 | 253 | PF10401 | 0.243 |
LIG_LIR_Apic_2 | 115 | 120 | PF02991 | 0.385 |
LIG_LIR_Apic_2 | 365 | 370 | PF02991 | 0.656 |
LIG_LIR_Apic_2 | 372 | 377 | PF02991 | 0.614 |
LIG_LIR_Apic_2 | 384 | 390 | PF02991 | 0.524 |
LIG_LIR_Apic_2 | 496 | 501 | PF02991 | 0.604 |
LIG_LIR_Gen_1 | 190 | 197 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 281 | 291 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 428 | 439 | PF02991 | 0.838 |
LIG_LIR_Nem_3 | 100 | 106 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 190 | 195 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 281 | 286 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 418 | 423 | PF02991 | 0.712 |
LIG_LIR_Nem_3 | 428 | 434 | PF02991 | 0.818 |
LIG_MYND_1 | 469 | 473 | PF01753 | 0.532 |
LIG_PCNA_yPIPBox_3 | 178 | 189 | PF02747 | 0.385 |
LIG_PROFILIN_1 | 499 | 505 | PF00235 | 0.491 |
LIG_REV1ctd_RIR_1 | 86 | 94 | PF16727 | 0.461 |
LIG_SH2_CRK | 117 | 121 | PF00017 | 0.385 |
LIG_SH2_CRK | 367 | 371 | PF00017 | 0.575 |
LIG_SH2_STAP1 | 160 | 164 | PF00017 | 0.243 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.263 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 497 | 500 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 527 | 530 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.418 |
LIG_SH3_1 | 497 | 503 | PF00018 | 0.593 |
LIG_SH3_1 | 51 | 57 | PF00018 | 0.435 |
LIG_SH3_3 | 214 | 220 | PF00018 | 0.385 |
LIG_SH3_3 | 328 | 334 | PF00018 | 0.789 |
LIG_SH3_3 | 349 | 355 | PF00018 | 0.761 |
LIG_SH3_3 | 385 | 391 | PF00018 | 0.696 |
LIG_SH3_3 | 467 | 473 | PF00018 | 0.546 |
LIG_SH3_3 | 496 | 502 | PF00018 | 0.658 |
LIG_SH3_3 | 51 | 57 | PF00018 | 0.435 |
LIG_SH3_3 | 526 | 532 | PF00018 | 0.656 |
LIG_SUMO_SIM_par_1 | 148 | 154 | PF11976 | 0.385 |
LIG_TRAF2_1 | 303 | 306 | PF00917 | 0.553 |
LIG_TRAF2_1 | 415 | 418 | PF00917 | 0.585 |
LIG_TRAF2_1 | 424 | 427 | PF00917 | 0.547 |
LIG_UBA3_1 | 181 | 189 | PF00899 | 0.385 |
LIG_WRC_WIRS_1 | 514 | 519 | PF05994 | 0.620 |
LIG_WW_1 | 524 | 527 | PF00397 | 0.492 |
LIG_WW_3 | 11 | 15 | PF00397 | 0.555 |
MOD_CDK_SPxxK_3 | 53 | 60 | PF00069 | 0.441 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.412 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.646 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.593 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.592 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.596 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.618 |
MOD_CK1_1 | 474 | 480 | PF00069 | 0.612 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.257 |
MOD_CK2_1 | 231 | 237 | PF00069 | 0.385 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.292 |
MOD_CK2_1 | 300 | 306 | PF00069 | 0.645 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.607 |
MOD_CK2_1 | 412 | 418 | PF00069 | 0.587 |
MOD_CK2_1 | 77 | 83 | PF00069 | 0.346 |
MOD_GlcNHglycan | 122 | 127 | PF01048 | 0.273 |
MOD_GlcNHglycan | 266 | 270 | PF01048 | 0.584 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.576 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.537 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.576 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.339 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.702 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.630 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.338 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.436 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.385 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.243 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.578 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.547 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.560 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.548 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.669 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.564 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.586 |
MOD_GSK3_1 | 509 | 516 | PF00069 | 0.599 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.340 |
MOD_N-GLC_1 | 231 | 236 | PF02516 | 0.309 |
MOD_N-GLC_1 | 4 | 9 | PF02516 | 0.560 |
MOD_N-GLC_1 | 484 | 489 | PF02516 | 0.703 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.243 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.508 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.456 |
MOD_NEK2_2 | 382 | 387 | PF00069 | 0.563 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.700 |
MOD_PIKK_1 | 369 | 375 | PF00454 | 0.573 |
MOD_PIKK_1 | 516 | 522 | PF00454 | 0.668 |
MOD_PK_1 | 282 | 288 | PF00069 | 0.543 |
MOD_PK_1 | 441 | 447 | PF00069 | 0.559 |
MOD_PK_1 | 97 | 103 | PF00069 | 0.314 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.563 |
MOD_PKA_2 | 440 | 446 | PF00069 | 0.556 |
MOD_Plk_1 | 21 | 27 | PF00069 | 0.774 |
MOD_Plk_1 | 213 | 219 | PF00069 | 0.243 |
MOD_Plk_1 | 231 | 237 | PF00069 | 0.309 |
MOD_Plk_1 | 339 | 345 | PF00069 | 0.580 |
MOD_Plk_1 | 382 | 388 | PF00069 | 0.562 |
MOD_Plk_2-3 | 231 | 237 | PF00069 | 0.385 |
MOD_Plk_2-3 | 241 | 247 | PF00069 | 0.292 |
MOD_Plk_4 | 307 | 313 | PF00069 | 0.567 |
MOD_Plk_4 | 382 | 388 | PF00069 | 0.565 |
MOD_Plk_4 | 393 | 399 | PF00069 | 0.543 |
MOD_Plk_4 | 441 | 447 | PF00069 | 0.559 |
MOD_Plk_4 | 493 | 499 | PF00069 | 0.548 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.489 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.472 |
MOD_ProDKin_1 | 304 | 310 | PF00069 | 0.583 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.763 |
MOD_ProDKin_1 | 359 | 365 | PF00069 | 0.734 |
MOD_ProDKin_1 | 425 | 431 | PF00069 | 0.753 |
MOD_ProDKin_1 | 469 | 475 | PF00069 | 0.615 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.436 |
MOD_SUMO_rev_2 | 161 | 166 | PF00179 | 0.243 |
TRG_DiLeu_BaLyEn_6 | 177 | 182 | PF01217 | 0.243 |
TRG_DiLeu_BaLyEn_6 | 48 | 53 | PF01217 | 0.415 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 192 | 195 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 431 | 434 | PF00928 | 0.693 |
TRG_ENDOCYTIC_2 | 527 | 530 | PF00928 | 0.504 |
TRG_NES_CRM1_1 | 68 | 81 | PF08389 | 0.423 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IU65 | Leishmania donovani | 67% | 100% |
E9AHQ6 | Leishmania infantum | 67% | 100% |
E9B477 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 100% |
Q4Q3U9 | Leishmania major | 66% | 100% |