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:0000139 | Golgi membrane | 5 | 1 |
GO:0005829 | cytosol | 2 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0032045 | guanyl-nucleotide exchange factor complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0034066 | Ric1-Rgp1 guanyl-nucleotide exchange factor complex | 4 | 1 |
GO:0098588 | bounding membrane of organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: A4HBC2
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0016197 | endosomal transport | 4 | 1 |
GO:0016482 | cytosolic transport | 4 | 1 |
GO:0042147 | retrograde transport, endosome to Golgi | 5 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 383 | 385 | PF00675 | 0.576 |
CLV_NRD_NRD_1 | 433 | 435 | PF00675 | 0.562 |
CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 383 | 385 | PF00082 | 0.552 |
CLV_PCSK_PC1ET2_1 | 134 | 136 | PF00082 | 0.614 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.423 |
DEG_APCC_DBOX_1 | 24 | 32 | PF00400 | 0.553 |
DEG_APCC_DBOX_1 | 277 | 285 | PF00400 | 0.706 |
DEG_APCC_DBOX_1 | 73 | 81 | PF00400 | 0.290 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.606 |
DEG_SPOP_SBC_1 | 175 | 179 | PF00917 | 0.533 |
DOC_CKS1_1 | 236 | 241 | PF01111 | 0.742 |
DOC_CKS1_1 | 336 | 341 | PF01111 | 0.388 |
DOC_CKS1_1 | 353 | 358 | PF01111 | 0.279 |
DOC_CKS1_1 | 394 | 399 | PF01111 | 0.596 |
DOC_MAPK_FxFP_2 | 401 | 404 | PF00069 | 0.354 |
DOC_MAPK_gen_1 | 190 | 197 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 190 | 197 | PF00069 | 0.495 |
DOC_MAPK_MEF2A_6 | 278 | 285 | PF00069 | 0.679 |
DOC_MAPK_MEF2A_6 | 69 | 77 | PF00069 | 0.555 |
DOC_PP1_RVXF_1 | 87 | 94 | PF00149 | 0.605 |
DOC_PP2B_LxvP_1 | 283 | 286 | PF13499 | 0.699 |
DOC_PP2B_LxvP_1 | 462 | 465 | PF13499 | 0.440 |
DOC_PP4_FxxP_1 | 145 | 148 | PF00568 | 0.448 |
DOC_PP4_FxxP_1 | 213 | 216 | PF00568 | 0.601 |
DOC_PP4_FxxP_1 | 401 | 404 | PF00568 | 0.507 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.702 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 352 | 357 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 393 | 398 | PF00397 | 0.593 |
DOC_WW_Pin1_4 | 439 | 444 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 450 | 455 | PF00397 | 0.467 |
LIG_14-3-3_CanoR_1 | 176 | 186 | PF00244 | 0.655 |
LIG_14-3-3_CanoR_1 | 25 | 34 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 257 | 263 | PF00244 | 0.702 |
LIG_14-3-3_CanoR_1 | 269 | 275 | PF00244 | 0.692 |
LIG_14-3-3_CanoR_1 | 278 | 284 | PF00244 | 0.701 |
LIG_14-3-3_CanoR_1 | 434 | 438 | PF00244 | 0.491 |
LIG_Actin_WH2_2 | 242 | 259 | PF00022 | 0.718 |
LIG_Actin_WH2_2 | 411 | 428 | PF00022 | 0.532 |
LIG_Clathr_ClatBox_1 | 80 | 84 | PF01394 | 0.514 |
LIG_EVH1_1 | 213 | 217 | PF00568 | 0.606 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.555 |
LIG_FHA_1 | 417 | 423 | PF00498 | 0.423 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.421 |
LIG_LIR_Apic_2 | 142 | 148 | PF02991 | 0.479 |
LIG_LIR_Apic_2 | 211 | 216 | PF02991 | 0.607 |
LIG_LIR_Apic_2 | 352 | 356 | PF02991 | 0.547 |
LIG_LIR_Apic_2 | 402 | 406 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 196 | 205 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 171 | 175 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 196 | 201 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 311 | 315 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 381 | 385 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 395 | 401 | PF02991 | 0.497 |
LIG_MYND_1 | 450 | 454 | PF01753 | 0.577 |
LIG_PAM2_1 | 450 | 462 | PF00658 | 0.330 |
LIG_PCNA_PIPBox_1 | 206 | 215 | PF02747 | 0.610 |
LIG_SH2_CRK | 382 | 386 | PF00017 | 0.330 |
LIG_SH2_NCK_1 | 136 | 140 | PF00017 | 0.604 |
LIG_SH2_PTP2 | 353 | 356 | PF00017 | 0.331 |
LIG_SH2_STAP1 | 136 | 140 | PF00017 | 0.594 |
LIG_SH2_STAP1 | 264 | 268 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 16 | 19 | PF00017 | 0.542 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 307 | 310 | PF00017 | 0.604 |
LIG_SH2_STAT5 | 353 | 356 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 398 | 401 | PF00017 | 0.539 |
LIG_SH3_2 | 466 | 471 | PF14604 | 0.654 |
LIG_SH3_3 | 211 | 217 | PF00018 | 0.547 |
LIG_SH3_3 | 233 | 239 | PF00018 | 0.622 |
LIG_SH3_3 | 245 | 251 | PF00018 | 0.685 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.440 |
LIG_SH3_3 | 391 | 397 | PF00018 | 0.583 |
LIG_SH3_3 | 460 | 466 | PF00018 | 0.462 |
LIG_SH3_3 | 84 | 90 | PF00018 | 0.492 |
LIG_SUMO_SIM_anti_2 | 347 | 352 | PF11976 | 0.515 |
LIG_SUMO_SIM_par_1 | 340 | 345 | PF11976 | 0.582 |
LIG_SUMO_SIM_par_1 | 427 | 433 | PF11976 | 0.288 |
LIG_SUMO_SIM_par_1 | 79 | 86 | PF11976 | 0.456 |
LIG_TRFH_1 | 213 | 217 | PF08558 | 0.606 |
LIG_WRC_WIRS_1 | 418 | 423 | PF05994 | 0.480 |
MOD_CDK_SPxK_1 | 235 | 241 | PF00069 | 0.481 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.545 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.352 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.694 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.607 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.583 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.482 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.629 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.466 |
MOD_CK1_1 | 433 | 439 | PF00069 | 0.270 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.460 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.759 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.617 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.671 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.729 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.614 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.529 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.491 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.411 |
MOD_GlcNHglycan | 57 | 61 | PF01048 | 0.741 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.520 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.586 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.697 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.527 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.533 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.424 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.368 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.651 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.684 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.528 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.646 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.594 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.632 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.572 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.309 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.771 |
MOD_N-GLC_1 | 322 | 327 | PF02516 | 0.638 |
MOD_N-GLC_1 | 363 | 368 | PF02516 | 0.438 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.524 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.700 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.565 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.692 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.582 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.594 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.502 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.461 |
MOD_NEK2_1 | 315 | 320 | PF00069 | 0.537 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.539 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.451 |
MOD_NEK2_1 | 437 | 442 | PF00069 | 0.544 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.527 |
MOD_NEK2_2 | 208 | 213 | PF00069 | 0.611 |
MOD_PIKK_1 | 273 | 279 | PF00454 | 0.574 |
MOD_PIKK_1 | 315 | 321 | PF00454 | 0.605 |
MOD_PIKK_1 | 35 | 41 | PF00454 | 0.731 |
MOD_PIKK_1 | 443 | 449 | PF00454 | 0.542 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.553 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.534 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.669 |
MOD_PKA_2 | 433 | 439 | PF00069 | 0.501 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.587 |
MOD_Plk_1 | 164 | 170 | PF00069 | 0.425 |
MOD_Plk_1 | 362 | 368 | PF00069 | 0.599 |
MOD_Plk_1 | 416 | 422 | PF00069 | 0.556 |
MOD_Plk_1 | 83 | 89 | PF00069 | 0.536 |
MOD_Plk_2-3 | 363 | 369 | PF00069 | 0.437 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.530 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.524 |
MOD_Plk_4 | 193 | 199 | PF00069 | 0.434 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.574 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.658 |
MOD_Plk_4 | 417 | 423 | PF00069 | 0.482 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.529 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.477 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.639 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.645 |
MOD_ProDKin_1 | 352 | 358 | PF00069 | 0.545 |
MOD_ProDKin_1 | 393 | 399 | PF00069 | 0.586 |
MOD_ProDKin_1 | 439 | 445 | PF00069 | 0.535 |
MOD_ProDKin_1 | 450 | 456 | PF00069 | 0.463 |
TRG_DiLeu_BaEn_1 | 76 | 81 | PF01217 | 0.508 |
TRG_DiLeu_BaLyEn_6 | 447 | 452 | PF01217 | 0.555 |
TRG_DiLeu_BaLyEn_6 | 457 | 462 | PF01217 | 0.426 |
TRG_ENDOCYTIC_2 | 382 | 385 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 398 | 401 | PF00928 | 0.341 |
TRG_ER_diArg_1 | 382 | 384 | PF00400 | 0.572 |
TRG_NES_CRM1_1 | 206 | 218 | PF08389 | 0.392 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I798 | Leptomonas seymouri | 56% | 100% |
A0A1X0PA91 | Trypanosomatidae | 22% | 100% |
A0A3Q8ILJ7 | Leishmania donovani | 76% | 100% |
A0A422NVD8 | Trypanosoma rangeli | 24% | 100% |
A4IAH0 | Leishmania infantum | 76% | 100% |
C9ZLS1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 100% |
E9B5J4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
Q4Q2E2 | Leishmania major | 74% | 100% |
V5BRG2 | Trypanosoma cruzi | 25% | 100% |