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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006457 | protein folding | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0061077 | chaperone-mediated protein folding | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0044183 | protein folding chaperone | 1 | 1 |
GO:0051082 | unfolded protein binding | 3 | 1 |
GO:0051087 | protein-folding chaperone binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 374 | 378 | PF00656 | 0.610 |
CLV_C14_Caspase3-7 | 394 | 398 | PF00656 | 0.618 |
CLV_MEL_PAP_1 | 113 | 119 | PF00089 | 0.415 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.398 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.288 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.681 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.775 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.583 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.743 |
CLV_PCSK_FUR_1 | 237 | 241 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 129 | 131 | PF00082 | 0.217 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.681 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.764 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.743 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.588 |
CLV_Separin_Metazoa | 385 | 389 | PF03568 | 0.339 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.625 |
DEG_SPOP_SBC_1 | 191 | 195 | PF00917 | 0.754 |
DEG_SPOP_SBC_1 | 369 | 373 | PF00917 | 0.477 |
DEG_SPOP_SBC_1 | 63 | 67 | PF00917 | 0.698 |
DOC_ANK_TNKS_1 | 254 | 261 | PF00023 | 0.542 |
DOC_CKS1_1 | 350 | 355 | PF01111 | 0.504 |
DOC_PP1_SILK_1 | 311 | 316 | PF00149 | 0.642 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.757 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.621 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.787 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.746 |
DOC_WW_Pin1_4 | 349 | 354 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 396 | 401 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.395 |
LIG_14-3-3_CanoR_1 | 115 | 124 | PF00244 | 0.297 |
LIG_14-3-3_CanoR_1 | 403 | 408 | PF00244 | 0.592 |
LIG_Actin_WH2_2 | 30 | 47 | PF00022 | 0.422 |
LIG_AP2alpha_1 | 219 | 223 | PF02296 | 0.488 |
LIG_BIR_III_2 | 80 | 84 | PF00653 | 0.407 |
LIG_BRCT_BRCA1_1 | 195 | 199 | PF00533 | 0.630 |
LIG_BRCT_BRCA1_1 | 34 | 38 | PF00533 | 0.497 |
LIG_DLG_GKlike_1 | 403 | 411 | PF00625 | 0.594 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.597 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.570 |
LIG_FHA_2 | 106 | 112 | PF00498 | 0.176 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.516 |
LIG_FHA_2 | 294 | 300 | PF00498 | 0.518 |
LIG_FHA_2 | 350 | 356 | PF00498 | 0.485 |
LIG_FHA_2 | 392 | 398 | PF00498 | 0.664 |
LIG_FHA_2 | 80 | 86 | PF00498 | 0.276 |
LIG_Integrin_RGD_1 | 212 | 214 | PF01839 | 0.443 |
LIG_LIR_Apic_2 | 426 | 430 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 118 | 128 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 111 | 117 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 118 | 124 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 333 | 338 | PF02991 | 0.459 |
LIG_Pex14_2 | 219 | 223 | PF04695 | 0.396 |
LIG_SH2_CRK | 206 | 210 | PF00017 | 0.637 |
LIG_SH2_CRK | 427 | 431 | PF00017 | 0.459 |
LIG_SH2_CRK | 72 | 76 | PF00017 | 0.276 |
LIG_SH2_CRK | 90 | 94 | PF00017 | 0.407 |
LIG_SH2_SRC | 384 | 387 | PF00017 | 0.628 |
LIG_SH2_SRC | 395 | 398 | PF00017 | 0.579 |
LIG_SH2_SRC | 413 | 416 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 413 | 416 | PF00017 | 0.610 |
LIG_SH3_3 | 270 | 276 | PF00018 | 0.549 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.590 |
LIG_SH3_3 | 325 | 331 | PF00018 | 0.484 |
LIG_SH3_3 | 334 | 340 | PF00018 | 0.358 |
LIG_SH3_3 | 342 | 348 | PF00018 | 0.421 |
LIG_SH3_3 | 350 | 356 | PF00018 | 0.469 |
LIG_TRAF2_1 | 82 | 85 | PF00917 | 0.295 |
LIG_WRPW_2 | 338 | 341 | PF00400 | 0.441 |
MOD_CDK_SPxxK_3 | 396 | 403 | PF00069 | 0.602 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.813 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.680 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.801 |
MOD_CK1_1 | 371 | 377 | PF00069 | 0.627 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.456 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.622 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.176 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.572 |
MOD_CK2_1 | 293 | 299 | PF00069 | 0.544 |
MOD_CK2_1 | 349 | 355 | PF00069 | 0.473 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.282 |
MOD_DYRK1A_RPxSP_1 | 166 | 170 | PF00069 | 0.649 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.741 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.670 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.777 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.605 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.596 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.550 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.582 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.666 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.749 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.734 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.600 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.780 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.623 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.565 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.542 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.484 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.441 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.576 |
MOD_NEK2_2 | 40 | 45 | PF00069 | 0.471 |
MOD_PIKK_1 | 361 | 367 | PF00454 | 0.668 |
MOD_PKA_1 | 115 | 121 | PF00069 | 0.433 |
MOD_PKA_1 | 184 | 190 | PF00069 | 0.736 |
MOD_PKA_1 | 48 | 54 | PF00069 | 0.717 |
MOD_PKA_2 | 115 | 121 | PF00069 | 0.433 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.744 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.402 |
MOD_PKA_2 | 48 | 54 | PF00069 | 0.719 |
MOD_PKB_1 | 182 | 190 | PF00069 | 0.812 |
MOD_Plk_1 | 365 | 371 | PF00069 | 0.656 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.428 |
MOD_Plk_2-3 | 224 | 230 | PF00069 | 0.523 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.530 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.788 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.550 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.743 |
MOD_ProDKin_1 | 349 | 355 | PF00069 | 0.502 |
MOD_ProDKin_1 | 396 | 402 | PF00069 | 0.676 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.395 |
MOD_SUMO_rev_2 | 221 | 228 | PF00179 | 0.449 |
MOD_SUMO_rev_2 | 80 | 89 | PF00179 | 0.327 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 72 | 75 | PF00928 | 0.276 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.407 |
TRG_ER_diArg_1 | 114 | 116 | PF00400 | 0.433 |
TRG_ER_diArg_1 | 128 | 131 | PF00400 | 0.441 |
TRG_ER_diArg_1 | 182 | 184 | PF00400 | 0.698 |
TRG_ER_diArg_1 | 204 | 206 | PF00400 | 0.597 |
TRG_ER_diArg_1 | 237 | 240 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 48 | 50 | PF00400 | 0.735 |
TRG_Pf-PMV_PEXEL_1 | 226 | 230 | PF00026 | 0.554 |
TRG_Pf-PMV_PEXEL_1 | 73 | 78 | PF00026 | 0.347 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I8S6 | Leptomonas seymouri | 61% | 100% |
A0A0S4JEE6 | Bodo saltans | 32% | 100% |
A0A1X0P2B2 | Trypanosomatidae | 36% | 100% |
A0A3Q8IFJ9 | Leishmania donovani | 89% | 100% |
A0A3R7P4U9 | Trypanosoma rangeli | 37% | 100% |
A4HI58 | Leishmania braziliensis | 82% | 99% |
A4I5D4 | Leishmania infantum | 89% | 100% |
C9ZQR6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
Q4Q7K0 | Leishmania major | 87% | 100% |
V5BPN3 | Trypanosoma cruzi | 35% | 100% |